A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185824



Internal ID20752864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62220975..62849523hg38UCSC Ensembl
chr15:62513174..63141722hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38628549
hg19628549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507845
Supporting Variants
Samples
Known GenesMGC15885, MIR190A, MIR6085, MIR8067, TLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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